Pharmacoeconomics Principles And Best Practices A Practical Guide
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Author | : Francisco Nuno Rocha Goncalves |
Publisher | : |
Total Pages | : 282 |
Release | : 2020-10-28 |
Genre | : Business & Economics |
ISBN | : 9780578793962 |
Pharmacoeconomics Principles and Best Practices: A Practical Guide is the product of collaborative efforts among multidisciplinary experts from different healthcare sectors. The Guide tackles many practical issues related to pharmacoeconomics that are of great importance to healthcare providers, policy and decision makers, and healthcare leaders. We hope the readers will find the Guide beneficial, and we welcome any feedback or comments.Editors: - Abdul Rahman Jazieh, MD, MPH- Francisco Nuno Rocha Goncalves, PhD- Laszlo Gulacsi, PhD- Nada Abu-Shraie, PharmD- Omar Da'ar, PhDChapters:1. "Introduction to Health Economics and Pharmacoeconomics" by Omar Da'ar2. "Models of Pharmacoeconomic Analysis" by Omar Da'ar3. "Assessments of Healthcare Costs" by Bander Balkhi, Ali Alhammad, and Laszlo Gulacsi4. "Guidelines for Pharmacoeconomic Evaluations" by Hana Al-Abdulkarim and Zsombor Zrubka5. "Optimization of Healthcare Expenditures at a National Level" by Ahmed Hamdan Al-jedai and Hajer Yousef Almudaiheem6. "The Pharmacy and Therapeutics Committee" by Nada Abu-Shraie7. "The Formulary Management System" by Nada Abu-Shraie8. "The Drug Evaluation Process: Clinical Evaluation" by Laila Carolina Abu EsbaNote - Supplemental Material is available at https: //innovativehci.com/en/page/books9. "Quality Improvement and Medication Utilization Review Process" by Mansoor Ahmed Khan, Abrar Al-Subhi, Eman Youssif and Sherin Ismail10. "Access to Quality Therapeutics in Cancer Care - Physician's Perspective" by Khalid AlSaleh and Nazia Sadaf11. "Role of Pharmaceutical Companies in Pharmacoeconomics" by Francisco Nuno Rocha Gonçalves and Muneera Al Majed12. "Generic Medications" by Hani Al Hashmi and Hamdi ElSoudi
Author | : Renee J. G. Arnold |
Publisher | : CRC Press |
Total Pages | : 259 |
Release | : 2016-04-19 |
Genre | : Medical |
ISBN | : 1420084402 |
The pharmaceutical industry is almost boundless in its ability to supply new drug therapies, but how does one decide which are the best medicines to use within restricted budgets? With particular emphasis on modeling, methodologies, data sources, and application to real-world dilemmas, Pharmacoeconomics: From Theory to Practice provides an introduc
Author | : Karen Rascati |
Publisher | : Lippincott Williams & Wilkins |
Total Pages | : 313 |
Release | : 2013-11-14 |
Genre | : Medical |
ISBN | : 146984186X |
"This new text is designed for a student or practitioner who is unfamiliar with "pharmacoeconomics." It provides a straightforward explanation of the essential pharmacoeconomics topics outlined by The Accreditation Council for Pharmacy Education (ACPE). It defines terminology used in research and covers the application of economic-based evaluation methods for pharmaceutical products and services. Users will find examples of how pharmacoeconomic evaluations relate to decisions that affect patient care and health-related quality of life"--Provided by publisher.
Author | : William F. McGhan |
Publisher | : |
Total Pages | : 172 |
Release | : 1991 |
Genre | : Medical |
ISBN | : |
Author | : Patrick M. Malone |
Publisher | : McGraw Hill Professional |
Total Pages | : 907 |
Release | : 2010-05-12 |
Genre | : Medical |
ISBN | : 0071492038 |
Extensive coverage of the Internet as a source of and distribution means for drug information, and detailed sections on evaluating medical literature from clinical trials Audience includes Pharmacists, Pharmacy students and Pharmacy schools Updated to include using PDAs for medication information Covers the ethical and legal aspects of drug information management Nothing else like it on the market
Author | : Agency for Healthcare Research and Quality/AHRQ |
Publisher | : Government Printing Office |
Total Pages | : 385 |
Release | : 2014-04-01 |
Genre | : Medical |
ISBN | : 1587634333 |
This User’s Guide is intended to support the design, implementation, analysis, interpretation, and quality evaluation of registries created to increase understanding of patient outcomes. For the purposes of this guide, a patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure, and that serves one or more predetermined scientific, clinical, or policy purposes. A registry database is a file (or files) derived from the registry. Although registries can serve many purposes, this guide focuses on registries created for one or more of the following purposes: to describe the natural history of disease, to determine clinical effectiveness or cost-effectiveness of health care products and services, to measure or monitor safety and harm, and/or to measure quality of care. Registries are classified according to how their populations are defined. For example, product registries include patients who have been exposed to biopharmaceutical products or medical devices. Health services registries consist of patients who have had a common procedure, clinical encounter, or hospitalization. Disease or condition registries are defined by patients having the same diagnosis, such as cystic fibrosis or heart failure. The User’s Guide was created by researchers affiliated with AHRQ’s Effective Health Care Program, particularly those who participated in AHRQ’s DEcIDE (Developing Evidence to Inform Decisions About Effectiveness) program. Chapters were subject to multiple internal and external independent reviews.
Author | : Brenda Waning |
Publisher | : |
Total Pages | : 209 |
Release | : 2001 |
Genre | : Medical |
ISBN | : 9780071355070 |
The not-to-be-missed, benchmark volume on the growing area of stud in the PharmD pharmacy curriculum. Provides a foundation for assessing the nature and extent of drug-taking behaviors. Text is adapted from the author's self-paced learning modules, developed for the Massachusetts College of Pharmacy.
Author | : David A. Holdford |
Publisher | : ASHP |
Total Pages | : 416 |
Release | : 2010-07-20 |
Genre | : Medical |
ISBN | : 1585282928 |
Written by leaders and experts in hospital and health-system practices and published by ASHP, the voice of the health-system pharmacy profession, Introduction to Hospital and Health-System Pharmacy Practice is required reading for students and practitioners alike. It’s a comprehensive manual for institutional pharmacy: legal and regulatory issues, medication safety, informatics, and more. Straightforward definitions and clear explanations provide a basic foundation for on-the-job training in hospitals and health-systems. It’s the only introductory textbook available in institutional pharmacy practice.This practical guide offers a highly readable introduction to key areas of pharmacy practice, including: Managing medication use Managing medication distribution Using technology in health systems Budgeting & finance responsibilities Administering and prepping sterile products Managing people Training options for careers Each chapter presents learning objectives and answers the “so what?” so common among student questions. Chapter reviews, discussion guidelines, key word definitions and interactive exercises augment the learning process.Written by hospital pharmacists for future hospital pharmacists, it’s everything important you need to know from the name you trust.For additional product resources about this publication, visit www.ashp.org/pharmacypractice
Author | : Agency for Health Care Research and Quality (U.S.) |
Publisher | : Government Printing Office |
Total Pages | : 236 |
Release | : 2013-02-21 |
Genre | : Medical |
ISBN | : 1587634236 |
This User’s Guide is a resource for investigators and stakeholders who develop and review observational comparative effectiveness research protocols. It explains how to (1) identify key considerations and best practices for research design; (2) build a protocol based on these standards and best practices; and (3) judge the adequacy and completeness of a protocol. Eleven chapters cover all aspects of research design, including: developing study objectives, defining and refining study questions, addressing the heterogeneity of treatment effect, characterizing exposure, selecting a comparator, defining and measuring outcomes, and identifying optimal data sources. Checklists of guidance and key considerations for protocols are provided at the end of each chapter. The User’s Guide was created by researchers affiliated with AHRQ’s Effective Health Care Program, particularly those who participated in AHRQ’s DEcIDE (Developing Evidence to Inform Decisions About Effectiveness) program. Chapters were subject to multiple internal and external independent reviews. More more information, please consult the Agency website: www.effectivehealthcare.ahrq.gov)
Author | : Institute of Medicine |
Publisher | : National Academies Press |
Total Pages | : 217 |
Release | : 2011-06-16 |
Genre | : Medical |
ISBN | : 030921646X |
Advances in medical, biomedical and health services research have reduced the level of uncertainty in clinical practice. Clinical practice guidelines (CPGs) complement this progress by establishing standards of care backed by strong scientific evidence. CPGs are statements that include recommendations intended to optimize patient care. These statements are informed by a systematic review of evidence and an assessment of the benefits and costs of alternative care options. Clinical Practice Guidelines We Can Trust examines the current state of clinical practice guidelines and how they can be improved to enhance healthcare quality and patient outcomes. Clinical practice guidelines now are ubiquitous in our healthcare system. The Guidelines International Network (GIN) database currently lists more than 3,700 guidelines from 39 countries. Developing guidelines presents a number of challenges including lack of transparent methodological practices, difficulty reconciling conflicting guidelines, and conflicts of interest. Clinical Practice Guidelines We Can Trust explores questions surrounding the quality of CPG development processes and the establishment of standards. It proposes eight standards for developing trustworthy clinical practice guidelines emphasizing transparency; management of conflict of interest ; systematic review-guideline development intersection; establishing evidence foundations for and rating strength of guideline recommendations; articulation of recommendations; external review; and updating. Clinical Practice Guidelines We Can Trust shows how clinical practice guidelines can enhance clinician and patient decision-making by translating complex scientific research findings into recommendations for clinical practice that are relevant to the individual patient encounter, instead of implementing a one size fits all approach to patient care. This book contains information directly related to the work of the Agency for Healthcare Research and Quality (AHRQ), as well as various Congressional staff and policymakers. It is a vital resource for medical specialty societies, disease advocacy groups, health professionals, private and international organizations that develop or use clinical practice guidelines, consumers, clinicians, and payers.